A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis-ichthyosis-deafness (KID) syndrome
Uffe Koppelhus, L Tranebjaerg, G Esberg, M Ramsing, M Lodahl, N D Rendtorff, H V Olesen, Mette Sommerlund, Uffe Koppelhus, L Tranebjaerg, Gitte Esberg, M Ramsing, Marianne Lodahl, Nanna Dahl Rendtorff, H V Olesen, Mette Sommerlund
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